EVERLIT SURVIVAL IODINE PREP PADS

Manufacturer
EVERLIT GLOBAL INC. | Changzhou Maokang Medical Products Co., Ltd
Effective date
2026-01-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:34:34

Label at a glance#

ProductEVERLIT SURVIVAL IODINE PREP PADS
Active ingredientPOVIDONE-IODINE
Label structure7 sections

Indications and uses

Topical antimicrobial agent for wound disinfection

Dosage and administration

Tear open the packet, use iodine saturated pad to cleanse desired skin area. Discard pad appropriately after use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Povidone Iodine USP 10%

Purpose

OTC - PURPOSE SECTION

Antiseptic for wound disinfection

Uses

INDICATIONS & USAGE SECTION

Topical antimicrobial agent for wound disinfection

Warnings

WARNINGS SECTION

Avoid contact with eyes. If happens, rinse thoroughly with water

For External Use Only.

If pain, redness, swelling, or infection develops, discontinue use and consult a phsician

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental swallowing, seek medical help or contact a Poison Control Center immediately

Other Information

OTHER SAFETY INFORMATION

Store at room temperature

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Citric acid, Glucoside, Hydroxyethyl cellulose, Nonoxynol-10, Glycerin, Soidium hydroxide, Potassium iodine, Purified water

Directions

DOSAGE & ADMINISTRATION SECTION

Tear open the packet, use iodine saturated pad to cleanse desired skin area. Discard pad appropriately after use.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NANA

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797730povidone-iodine 10 % Medicated PadPSN3
797730povidone-iodine 100 MG/ML Medicated PadSCD3
797730povidone-iodine 10 % (titratable iodine 1 % ) Medicated PadSY3
797730povidone-iodine 10 % Medicated PadSY3
797730povidone-iodine 10 % Medicated SwabstickSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83807-023-01EVERLIT SURVIVAL IODINE PREP PADS1 in 1 PACKETCLOTH13

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83807-02383807-023-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-12-16monthly-update2026-06-03 17:46:06

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
EVERLIT SURVIVAL IODINE PREP PADSPOVIDONE-IODINEEVERLIT GLOBAL INC.3a03fc8d-2653-9183-e063-6294a90ad76e2026-01-23WarningsExact identifier
ndc (package): 83807-023-01
ndc (product): 83807-023
ndc11 (package): 83807002301
spl id: 49120f89-68c1-0bb8-e063-6294a90a0b98
spl set id: 3a03fc8d-2653-9183-e063-6294a90ad76e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.